Non-Invasive Epigenetic Profiling of Cell Free Fetal DNA: Markers of Common Prenatal Exposures that Shape the Risk for Neurodevelopmental Disorders and Autism Spectrum Disorders

无细胞胎儿 DNA 的非侵入性表观遗传分析：影响神经发育障碍和自闭症谱系障碍风险的常见产前暴露标记

• 批准号: 392406
• 负责人: Laufer Benjamin
• 金额: $ 10.2万
• 依托单位: University of California (Davis)
• 依托单位国家: 加拿大
• 项目类别: Fellowship Programs
• 财政年份: 2018
• 资助国家: 加拿大
• 起止时间: 2018-09-01 至 2020-09-01
• 项目状态: 已结题
• 来源: https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=392406&lang=en
• 关键词: Autism Spectrum Disorders (Asds); Cell Free Fetal Dna; Dna Methylation; Epigenomics; Indigenous Peoples In Canada; Neurodevelopmental Disorders (Ndds); Obesity; Placenta; Polychlorinated Biphenyls (Pcbs); Prenatal Exposures

This research impacts Indigenous Peoples. Exposures to negative environmental conditions during pregnancy increase the risk for neurodevelopmental disorders (NDDs), which include Autism Spectrum Disorders (ASDs). These exposures represent a public health

这项研究影响到土著人民。 怀孕期间暴露于负面环境条件会增加神经发育障碍（NDD）的风险，其中包括自闭症谱系障碍（ASD）。这些暴露代表了一种公共健康